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dc.contributor.advisorMatoušek, Jaroslav
dc.contributor.authorSelinger, Martin
dc.date.accessioned2021-12-06T14:05:48Z
dc.date.available2021-12-06T14:05:48Z
dc.date.issued2013
dc.date.submitted2013-04-26
dc.identifier.urihttps://dspace.jcu.cz/handle/20.500.14390/24496
dc.format59
dc.format59
dc.language.isocze
dc.publisherJihočeská univerzitacze
dc.rightsBez omezení
dc.subjectPotato spindle tuber viroid (PSTVd)eng
dc.subjectPTGSeng
dc.subjectvsRNAeng
dc.subjectleaf factoryeng
dc.subjectSl-MYBeng
dc.titleStudium exprese cílových mRNA při pospiviroidní patogenezi v systému "leaf factory"cze
dc.title.alternativeExpression of target mRNAs during Popsipviroid pathogenesis in the "leaf factory" systemeng
dc.typediplomová prácecze
dc.identifier.stag27827
dc.description.abstract-translatedThe aim of this work was to identify potential mRNA targets of PTGS triggered by viroid-derived small RNAs (vsRNAs) in PSTVd-infected tomato plants (S. lycopersicum L.). We selected 47 possible gene targets using data provided by Prof. Dr. Steger (Heinrich Heine Universität, Düsseldorf, Germany) - the list of 1633 possible target mRNAs from tomato based on vsRNA:mRNA duplex prediction. The vsRNA sequences were obtained by Illumina sequencing of small RNA libraries from healthy and PSTVd-infected tomato plants. By qRT-PCR analysis we identified 6 genes with significantly altered levels of mRNA in PSTVd-infected tomato plants: CUL1 (protein ubiquitination), ERF4 (transcription factor of abiotic stress signalling pathway), H/ACA1 (rRNA pseudouridylation), NPH3 (transcription factor of fototropic signalling pathway), Sl-MYB (transcription factor regulating leaf development) and TCP3 (transcription factor regulating leaf development). The binary vector pLV07 with inserted expression cassette containing coding sequence of Sl-MYB was prepared for experiments in ?leaf factory? system in N. benthamiana plants. Expression analyses in ?leaf factory? system after 1,5 DPI using qRT-PCR and RNA blots revealed strong inhibition of expression of Sl-MYB in leaf sectors infiltrated with severe PSTVd AS1 strain, while mild PSTVd QFA strain showed minimal change in expression comparing to control sectors. Moreover, the overexpression of Sl-MYB in leaf sectors resulted in development of necroses after 2,5-3 DPI, in presence of silencing suppressor p19 after 2 DPI. The development of necroses was largely inhibited in PSTVd AS1-infiltrated leaf sectors in comparison with PSTVd QFA- and control-infiltrated sectors.eng
dc.date.accepted2013-05-28
dc.description.departmentPřírodovědecká fakultacze
dc.thesis.degree-disciplineExperimentální biologie - specializace Genetika a genové inženýrstvícze
dc.thesis.degree-grantorJihočeská univerzita. Přírodovědecká fakultacze
dc.thesis.degree-nameMgr.
dc.thesis.degree-programBiologiecze
dc.description.gradeDokončená práce s úspěšnou obhajoboucze
dc.contributor.refereePetrzik, Karel
dc.contributor.refereeVlasák, Josef


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